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Alginate anticorps

Cet anticorps anti- est un anticorps Souris Monoclonal détectant dans ELISA. Adapté pour Pseudomonas.
N° du produit ABIN7489925

Aperçu rapide pour Alginate anticorps (ABIN7489925)

Antigène

Alginate

Reactivité

Pseudomonas

Hôte

  • 10
Souris

Clonalité

  • 10
Monoclonal

Conjugué

  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Inconjugué

Application

  • 10
  • 10
ELISA

Clone

3G4-1F5
  •  Réactivité croisée

    Pseudomonas

    Immunogène

    Sodium alginate conjugated to KLH

    Isotype

    IgG1
  • Indications d'application

    ELISA: Use at 0.5-20 μg/mL with alginate on the solid phase. Working concentrations for these antibodies are dependent on the purity and concentration of alginate in samples tested.

    Commentaires

    Anti-Alginate Mouse Monoclonal Antibody

    Restrictions

    For Research Use only
  • Format

    Liquid

    Reconstitution

    Dilute in PBS or medium that is identical to that used in the assay system.

    Concentration

    Lot specific

    Buffer

    50 % Glycerol,PBS, pH 7.4, 50 % glycerol, 0.1 % sodium azide.,Phosphate Buffered Saline

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    These antibodies are stable for at least one (1) year at -20°C. Store in appropriate aliquots to avoid multiple freeze-thaw cycles.
  • Antigène

    Alginate

    Classe de substances

    Chemical

    Sujet

    Pulmonary infection by mucoid, alginate-producing Pseudomonas aeruginosa is the leading cause of mortality among patients suffering from cystic fibrosis. During early childhood, cystic fibrosis patients are colonized by multiple bacterial pathogens including nonmucoid P. aeruginosa. The appearance of mucoid isolates indicates progression to chronic infections. Recent evidence indicates that P. aeruginosa is most resistant to antibiotics when the infecting cells are present as a biofilm, as they appear to be in the lungs of cystic fibrosis patients.
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